A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2725659



Internal ID17737025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122450..135072hg38UCSC Ensembl
Innerchr9:122450..135072hg19UCSC Ensembl
Innerchr9:112450..125072hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3812623
hg1912623
hg1812623
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982361
Supporting Variants
SamplesHGDP00456
Known GenesCBWD1
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2725659
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer